International Medical Devices Database

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here

Type of Event
Recall
Date
2008-05-22
Event Country
France
Event Source
ANSM
Event Source URL
https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/retrait-de-lots-d-obturateurs-bd-venflon-bd-insyte-et-bd-adsyte-pro-de-la-societe-becton-dickinson
Notes / Alerts

French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and France.
Extra notes in the data
Action
On May 21, 2008, BECTON DICKINSON withdrew from the market the batches of the references specified in the attached recall message, of the medical device known as "BD Venflon, BD Insyte and BD Adsyte Pro shutters", following a report reporting the presence of slots and / or holes on some individual packages. The company BECTON DICKINSON has directly notified the recipients of the incriminated lots with the message attached (21/05/2008) (35 KB) validated by Afssaps. This information is addressed to the directors and correspondents of materiovigilance for diffusion if necessary to the services concerned. The relevant European Competent Authorities are informed of this measure by the manufacturer.

Device

BD Venflon, BD Insyte and BD Adsyte Pro shutter batches

Model / Serial
Product Description
medical_device
Manufacturer
BECTON DICKINSON

Manufacturer

BECTON DICKINSON

Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
LAANSM

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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Recall of BD Venflon, BD Insyte and BD Adsyte Pro shutter batches

What is this?

Device

BD Venflon, BD Insyte and BD Adsyte Pro shutter batches

Manufacturer

BECTON DICKINSON